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Structure of 13719-61-4
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2-Chloro-5-methoxybenzaldehyde features a chlorine atom at the ortho position and a methoxy group at the para position relative to the aldehyde, creating a uniquely electron-deficient aromatic scaffold. This configuration enhances reactivity in electrophilic substitution and facilitates coupling reactions under mild conditions. The aldehyde functionality enables direct incorporation into complex molecular architectures via imine formation or reductive amination. Its bench-stable nature supports reliable handling in synthetic workflows.
2-Chloro-5-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles and biologically active scaffolds. Its electron-withdrawing chlorine and methoxy groups provide orthogonal reactivity for selective functionalization, while the aldehyde functionality facilitates imine formation, reductive amination, and coupling reactions. Bench-stable and amenable to standard purification techniques, it functions reliably in multistep synthetic sequences.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: